A 40-year-old male patient presented with sudden-onset persistent chest pain accompanied by widespread anterior ST-segment elevation on electrocardiogram (ECG). Initially diagnosed as acute myocardial infarction (AMI)
he received dual antiplatelet therapy. However
a combination of clues including bilateral blood pressure asymmetry
rapid ST-segment resolution
negative troponin but strikingly elevated plasma D-dimer (>10
000 ng/mL) raised a high suspicion of acute aortic syndrome. Aortic computed tomography angiography (CTA) confirmed Stanford type A aortic dissection involving the left main coronary artery ostium. The patient underwent successful surgical repair. Acute aortic dissection(AAD)
particularly type A
is a life-threatening cardiovascular emergency. Its clinical presentation often overlaps with acute coronary syndrome (ACS)
leading to misdiagnosis
inappropriate antiplatelet therapy
and increased risk of catastrophic hemorrhage and mortality. The 2024 ESC guidelines recommend a multi-parameter diagnostic strategy combining the Aortic Dissection Detection Risk Score (ADD-RS) and D-dimer testing for efficient patient triage. For patients with low clinical risk
a negative D-dimer can effectively rule out dissection; for those with intermediate to high clinical risk
immediate confirmatory imaging is required to avoid diagnostic delay. Implementing a standardized early recognition algorithm for patients with chest pain is paramount to preventing fatal delays and improving outcomes in patients with type A aortic dissection.
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references
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